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Tamar Harel

Showing results (11-20 of 113) with videos related to

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Tissue Engineering|June 15, 2006
Enhancing the drug metabolism activities of C3A--a human hepatocyte cell line--by tissue engineering within alginate scaffoldsTsiona Elkayam, Sigalit Amitay-Shaprut, Mona Dvir-Ginzberg, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 14, 2024
Genetics of bilateral pediatric cataract in the Israeli and Palestinian populationsClaudia Yahalom, Irene Anteby, Karen Hendler, et al.
American Journal of Medical Genetics. Part A|July 8, 2017
Homozygous null variant in CRADD, encoding an adaptor protein that mediates apoptosis, is associated with lissencephalyTamar Harel, Nuphar Hacohen, Avraham Shaag, et al.
American Journal of Medical Genetics. Part A|September 11, 2019
Homozygous variants in MAPRE2 and CDON in individual with skin folds, growth delay, retinal coloboma, and pyloric stenosisLina Berkun, Mordechai Slae, Hagar Mor-Shaked, et al.
Human Genetics|July 17, 2004
CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindredsUdy Bar-Yosef, Izzeldin Abuelaish, Tamar Harel, et al.
European Journal of Human Genetics : EJHG|October 3, 2003
Limb-girdle muscular dystrophy 2I: phenotypic variability within a large consanguineous Bedouin family associated with a novel FKRP mutationTamar Harel, Yael Goldberg, Stavit A Shalev, et al.
Parkinsonism & Related Disorders|July 14, 2024
Low prevalence of SCA27B in adult-onset cerebellar ataxia cohort of Jewish ancestryOrli Halstuk, Roy Dayan, Shira Silverstein, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2011
Modulation of cardiac macrophages by phosphatidylserine-presenting liposomes improves infarct repairTamar Harel-Adar, Tamar Ben Mordechai, Yoram Amsalem, et al.
Journal of Molecular Endocrinology|October 3, 2025
Intronic IGF1R variant causing aberrant splicing, short stature, and neurological impairmentsLiya Kerem, Jonathan Rips, Adam Zaretsky, et al.
Tissue Engineering. Part A|December 25, 2012
Cutaneous wound healing after treatment with plant-derived human recombinant collagen flowable gelShani Shilo, Sigal Roth, Tal Amzel, et al.
Pageof 12

Showing results (11-20 of 113) with videos related to

Sort By:
Pageof 12
Tissue Engineering|June 15, 2006
Enhancing the drug metabolism activities of C3A--a human hepatocyte cell line--by tissue engineering within alginate scaffoldsTsiona Elkayam, Sigalit Amitay-Shaprut, Mona Dvir-Ginzberg, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 14, 2024
Genetics of bilateral pediatric cataract in the Israeli and Palestinian populationsClaudia Yahalom, Irene Anteby, Karen Hendler, et al.
American Journal of Medical Genetics. Part A|July 8, 2017
Homozygous null variant in CRADD, encoding an adaptor protein that mediates apoptosis, is associated with lissencephalyTamar Harel, Nuphar Hacohen, Avraham Shaag, et al.
American Journal of Medical Genetics. Part A|September 11, 2019
Homozygous variants in MAPRE2 and CDON in individual with skin folds, growth delay, retinal coloboma, and pyloric stenosisLina Berkun, Mordechai Slae, Hagar Mor-Shaked, et al.
Human Genetics|July 17, 2004
CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindredsUdy Bar-Yosef, Izzeldin Abuelaish, Tamar Harel, et al.
European Journal of Human Genetics : EJHG|October 3, 2003
Limb-girdle muscular dystrophy 2I: phenotypic variability within a large consanguineous Bedouin family associated with a novel FKRP mutationTamar Harel, Yael Goldberg, Stavit A Shalev, et al.
Parkinsonism & Related Disorders|July 14, 2024
Low prevalence of SCA27B in adult-onset cerebellar ataxia cohort of Jewish ancestryOrli Halstuk, Roy Dayan, Shira Silverstein, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2011
Modulation of cardiac macrophages by phosphatidylserine-presenting liposomes improves infarct repairTamar Harel-Adar, Tamar Ben Mordechai, Yoram Amsalem, et al.
Journal of Molecular Endocrinology|October 3, 2025
Intronic IGF1R variant causing aberrant splicing, short stature, and neurological impairmentsLiya Kerem, Jonathan Rips, Adam Zaretsky, et al.
Tissue Engineering. Part A|December 25, 2012
Cutaneous wound healing after treatment with plant-derived human recombinant collagen flowable gelShani Shilo, Sigal Roth, Tal Amzel, et al.
Pageof 12